FDA-Device2025-04-02Class II
Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS
Baxter Healthcare Corporation
Hazard
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket. A gasket failure could lead to potential fluid ingress due to cleaning, or as a result of an IV fluid spill.
Sold states
US Nationwide distribution in the states of AR, CA, FL, IA, IN, LA, MO, MT, NC, NY, OH, OR, PA, TN, TX, VA, WA, WI, WV.
Affected count
149 units
Manufactured in
1 Baxter Pkwy, N/A, Deerfield, IL, United States
Products
Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1423-2025Don't want to check this manually?
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